 Naomi Meeks
Concepts (196)
Concepts are derived automatically from a person's publications.
Concepts are listed by decreasing relevance which is based on many factors, including how many publications the person wrote about that topic, how long ago those publications were written, and how many publications other people have written on that same topic.
| Name |
Number of Publications
|
Most Recent Publication
|
Publications by All Authors
|
Concept Score
|
Why?
|
|---|
| Intellectual Disability | 8 | 2024 | 183 | 0.940 |
Why?
| | Muscular Diseases | 1 | 2026 | 109 | 0.920 |
Why?
| | Actins | 1 | 2026 | 428 | 0.810 |
Why?
| | Dwarfism | 1 | 2023 | 14 | 0.780 |
Why?
| | Osteochondrodysplasias | 1 | 2023 | 18 | 0.770 |
Why?
| | Pseudohypoparathyroidism | 1 | 2022 | 3 | 0.720 |
Why?
| | Genetic Predisposition to Disease | 3 | 2026 | 2458 | 0.660 |
Why?
| | Cardiomyopathies | 1 | 2022 | 339 | 0.540 |
Why?
| | Hypopituitarism | 1 | 2015 | 16 | 0.440 |
Why?
| | Craniofacial Abnormalities | 3 | 2021 | 78 | 0.420 |
Why?
| | Cystinuria | 2 | 2024 | 3 | 0.410 |
Why?
| | Phenotype | 10 | 2026 | 3216 | 0.410 |
Why?
| | Autism Spectrum Disorder | 4 | 2020 | 425 | 0.390 |
Why?
| | Congenital Disorders of Glycosylation | 2 | 2026 | 17 | 0.390 |
Why?
| | Developmental Disabilities | 5 | 2021 | 284 | 0.380 |
Why?
| | Neurodevelopmental Disorders | 3 | 2022 | 236 | 0.380 |
Why?
| | Seizures | 3 | 2021 | 491 | 0.300 |
Why?
| | Genetic Testing | 3 | 2024 | 493 | 0.270 |
Why?
| | Adrenal Insufficiency | 2 | 2021 | 31 | 0.270 |
Why?
| | Mutation | 8 | 2026 | 4130 | 0.260 |
Why?
| | Amino Acid Transport Systems, Basic | 2 | 2024 | 4 | 0.250 |
Why?
| | Cystine | 2 | 2024 | 17 | 0.250 |
Why?
| | Fucose | 1 | 2026 | 7 | 0.230 |
Why?
| | Mutation, Missense | 2 | 2018 | 337 | 0.230 |
Why?
| | Monosaccharide Transport Proteins | 1 | 2026 | 56 | 0.230 |
Why?
| | Uterus | 1 | 2026 | 228 | 0.220 |
Why?
| | Dichloroacetic Acid | 1 | 2024 | 7 | 0.220 |
Why?
| | Acidosis, Lactic | 1 | 2024 | 46 | 0.210 |
Why?
| | Child, Preschool | 12 | 2026 | 12016 | 0.200 |
Why?
| | Glypicans | 1 | 2023 | 11 | 0.200 |
Why?
| | Heterozygote | 1 | 2024 | 317 | 0.200 |
Why?
| | Aggression | 1 | 2024 | 180 | 0.190 |
Why?
| | Growth Disorders | 1 | 2023 | 89 | 0.190 |
Why?
| | Whole Genome Sequencing | 2 | 2024 | 183 | 0.180 |
Why?
| | Face | 2 | 2022 | 176 | 0.180 |
Why?
| | Siblings | 1 | 2023 | 197 | 0.180 |
Why?
| | Chromogranins | 1 | 2022 | 13 | 0.180 |
Why?
| | GTP-Binding Protein alpha Subunits, Gs | 1 | 2022 | 9 | 0.180 |
Why?
| | Nervous System Malformations | 1 | 2022 | 46 | 0.180 |
Why?
| | Hedgehog Proteins | 1 | 2023 | 201 | 0.180 |
Why?
| | Humans | 30 | 2026 | 147293 | 0.170 |
Why?
| | Research Report | 1 | 2022 | 89 | 0.170 |
Why?
| | Channelopathies | 1 | 2011 | 5 | 0.170 |
Why?
| | Autistic Disorder | 1 | 2024 | 226 | 0.170 |
Why?
| | Segmental Duplications, Genomic | 1 | 2021 | 8 | 0.170 |
Why?
| | Infant | 8 | 2026 | 10194 | 0.170 |
Why?
| | Genomic Structural Variation | 1 | 2021 | 13 | 0.170 |
Why?
| | Williams Syndrome | 1 | 2021 | 13 | 0.160 |
Why?
| | Neurotransmitter Agents | 1 | 2011 | 84 | 0.160 |
Why?
| | Chromosome Disorders | 1 | 2021 | 47 | 0.160 |
Why?
| | Adrenal Hyperplasia, Congenital | 1 | 2021 | 39 | 0.160 |
Why?
| | N-Acetylglucosaminyltransferases | 1 | 2020 | 24 | 0.160 |
Why?
| | Evidence-Based Medicine | 1 | 2024 | 742 | 0.160 |
Why?
| | Neurogenesis | 1 | 2011 | 158 | 0.150 |
Why?
| | Facies | 1 | 2019 | 22 | 0.150 |
Why?
| | Male | 19 | 2026 | 73950 | 0.140 |
Why?
| | Spasms, Infantile | 1 | 2020 | 138 | 0.140 |
Why?
| | Aldehyde Dehydrogenase | 1 | 2019 | 99 | 0.140 |
Why?
| | cdc42 GTP-Binding Protein | 1 | 2018 | 21 | 0.130 |
Why?
| | Noonan Syndrome | 1 | 2018 | 14 | 0.130 |
Why?
| | Chromosomes, Human, Pair 15 | 3 | 2021 | 50 | 0.130 |
Why?
| | Genetic Variation | 2 | 2021 | 995 | 0.130 |
Why?
| | RNA Helicases | 1 | 2017 | 27 | 0.130 |
Why?
| | Genetic Heterogeneity | 1 | 2018 | 66 | 0.130 |
Why?
| | Farber Lipogranulomatosis | 1 | 2017 | 4 | 0.130 |
Why?
| | Conjunctival Diseases | 1 | 2017 | 23 | 0.130 |
Why?
| | Muscular Atrophy | 1 | 2018 | 87 | 0.130 |
Why?
| | Synovitis | 1 | 2017 | 35 | 0.120 |
Why?
| | Child | 10 | 2024 | 22979 | 0.120 |
Why?
| | Arthritis | 1 | 2017 | 97 | 0.120 |
Why?
| | Imaging, Three-Dimensional | 1 | 2020 | 587 | 0.120 |
Why?
| | Prader-Willi Syndrome | 1 | 2016 | 33 | 0.120 |
Why?
| | Abnormalities, Multiple | 1 | 2018 | 199 | 0.120 |
Why?
| | Premature Birth | 1 | 2020 | 390 | 0.120 |
Why?
| | Uveitis | 1 | 2017 | 151 | 0.110 |
Why?
| | Diabetes Insipidus | 1 | 2015 | 6 | 0.110 |
Why?
| | Holoprosencephaly | 1 | 2015 | 8 | 0.110 |
Why?
| | Energy Metabolism | 1 | 2011 | 936 | 0.110 |
Why?
| | Human Growth Hormone | 1 | 2015 | 47 | 0.110 |
Why?
| | Thyrotropin | 1 | 2015 | 120 | 0.110 |
Why?
| | Adolescent | 7 | 2024 | 22825 | 0.100 |
Why?
| | Hypogonadism | 1 | 2015 | 93 | 0.100 |
Why?
| | Amino Acid Transport Systems, Neutral | 2 | 2024 | 4 | 0.100 |
Why?
| | Epilepsy | 1 | 2019 | 399 | 0.100 |
Why?
| | Transcription Factors | 1 | 2021 | 1747 | 0.100 |
Why?
| | Repressor Proteins | 2 | 2021 | 429 | 0.090 |
Why?
| | Glycosylation | 2 | 2026 | 176 | 0.090 |
Why?
| | Heart Defects, Congenital | 1 | 2021 | 941 | 0.090 |
Why?
| | High-Throughput Nucleotide Sequencing | 1 | 2015 | 539 | 0.090 |
Why?
| | Female | 14 | 2026 | 80076 | 0.080 |
Why?
| | Sequence Deletion | 1 | 2011 | 192 | 0.080 |
Why?
| | Mosaicism | 1 | 2011 | 73 | 0.080 |
Why?
| | Gene Frequency | 2 | 2023 | 498 | 0.080 |
Why?
| | Frameshift Mutation | 1 | 2010 | 32 | 0.080 |
Why?
| | Proteins | 1 | 2016 | 1024 | 0.080 |
Why?
| | Exons | 1 | 2011 | 365 | 0.080 |
Why?
| | Chromosome Mapping | 3 | 2022 | 512 | 0.070 |
Why?
| | HEK293 Cells | 2 | 2024 | 745 | 0.070 |
Why?
| | Brain | 1 | 2011 | 3009 | 0.070 |
Why?
| | Syndrome | 3 | 2020 | 385 | 0.070 |
Why?
| | Ubiquitin-Protein Ligases | 1 | 2010 | 199 | 0.070 |
Why?
| | Tandem Repeat Sequences | 1 | 2006 | 23 | 0.060 |
Why?
| | Repetitive Sequences, Nucleic Acid | 1 | 2006 | 118 | 0.060 |
Why?
| | Infertility, Male | 1 | 2006 | 82 | 0.060 |
Why?
| | Hearing Loss, Sensorineural | 1 | 2006 | 75 | 0.060 |
Why?
| | Autoimmune Diseases | 1 | 2010 | 471 | 0.060 |
Why?
| | Gene Deletion | 1 | 2006 | 392 | 0.050 |
Why?
| | Pyruvate Dehydrogenase (Lipoamide) | 1 | 2024 | 10 | 0.050 |
Why?
| | Infant, Newborn | 3 | 2024 | 6543 | 0.050 |
Why?
| | PDZ Domains | 1 | 2024 | 12 | 0.050 |
Why?
| | Amino Acid Transport System y+ | 1 | 2024 | 10 | 0.050 |
Why?
| | Genotype | 2 | 2020 | 1875 | 0.050 |
Why?
| | Sialoglycoproteins | 1 | 2024 | 157 | 0.050 |
Why?
| | Incidental Findings | 1 | 2024 | 82 | 0.050 |
Why?
| | Introns | 1 | 2024 | 260 | 0.050 |
Why?
| | Histone Demethylases | 1 | 2022 | 39 | 0.050 |
Why?
| | Alleles | 1 | 2026 | 909 | 0.050 |
Why?
| | Gene Expression | 2 | 2018 | 1481 | 0.040 |
Why?
| | Genetics, Population | 1 | 2023 | 226 | 0.040 |
Why?
| | Hypertelorism | 1 | 2021 | 1 | 0.040 |
Why?
| | Biomarkers | 2 | 2026 | 4351 | 0.040 |
Why?
| | Membrane Proteins | 2 | 2024 | 1171 | 0.040 |
Why?
| | Muscle Hypotonia | 1 | 2021 | 34 | 0.040 |
Why?
| | Dietary Supplements | 1 | 2026 | 586 | 0.040 |
Why?
| | Chromosome Breakpoints | 1 | 2021 | 9 | 0.040 |
Why?
| | Chromosomes, Human, Pair 16 | 1 | 2021 | 36 | 0.040 |
Why?
| | Genes, X-Linked | 1 | 2020 | 21 | 0.040 |
Why?
| | Nerve Tissue Proteins | 1 | 2024 | 597 | 0.040 |
Why?
| | Chromosome Deletion | 1 | 2021 | 127 | 0.040 |
Why?
| | Transferrin | 1 | 2020 | 50 | 0.040 |
Why?
| | Synapses | 1 | 2024 | 448 | 0.040 |
Why?
| | Adult | 5 | 2024 | 41405 | 0.040 |
Why?
| | Diet, Ketogenic | 1 | 2020 | 39 | 0.040 |
Why?
| | Chromosomal Proteins, Non-Histone | 1 | 2020 | 130 | 0.040 |
Why?
| | 2-Aminoadipic Acid | 1 | 2019 | 7 | 0.040 |
Why?
| | Molecular Sequence Annotation | 1 | 2019 | 109 | 0.040 |
Why?
| | Young Adult | 3 | 2024 | 14437 | 0.030 |
Why?
| | Phosphoproteins | 1 | 2021 | 337 | 0.030 |
Why?
| | Consanguinity | 2 | 2010 | 50 | 0.030 |
Why?
| | Critical Illness | 1 | 2024 | 907 | 0.030 |
Why?
| | Nuclear Proteins | 1 | 2022 | 745 | 0.030 |
Why?
| | Fluorometholone | 1 | 2017 | 4 | 0.030 |
Why?
| | Proteomics | 1 | 2024 | 1203 | 0.030 |
Why?
| | Hereditary Autoinflammatory Diseases | 1 | 2017 | 13 | 0.030 |
Why?
| | Prevalence | 1 | 2024 | 2889 | 0.030 |
Why?
| | Pedigree | 2 | 2010 | 522 | 0.030 |
Why?
| | Nod2 Signaling Adaptor Protein | 1 | 2017 | 34 | 0.030 |
Why?
| | Protein Structure, Secondary | 1 | 2018 | 372 | 0.030 |
Why?
| | Diagnosis, Differential | 1 | 2011 | 1518 | 0.030 |
Why?
| | Adenosine Triphosphatases | 1 | 2017 | 159 | 0.030 |
Why?
| | Genomic Imprinting | 1 | 2016 | 28 | 0.030 |
Why?
| | Intrinsically Disordered Proteins | 1 | 2016 | 45 | 0.030 |
Why?
| | Central Nervous System | 1 | 2017 | 282 | 0.030 |
Why?
| | Neurons | 1 | 2024 | 1672 | 0.030 |
Why?
| | Sarcoidosis | 1 | 2017 | 164 | 0.030 |
Why?
| | Base Sequence | 2 | 2010 | 2175 | 0.030 |
Why?
| | Child Development | 1 | 2019 | 484 | 0.030 |
Why?
| | Molecular Sequence Data | 2 | 2010 | 2886 | 0.030 |
Why?
| | Amino Acids | 1 | 2017 | 519 | 0.020 |
Why?
| | Gene Expression Regulation | 1 | 2022 | 2625 | 0.020 |
Why?
| | DNA-Binding Proteins | 1 | 2020 | 1488 | 0.020 |
Why?
| | Intracellular Signaling Peptides and Proteins | 1 | 2016 | 459 | 0.020 |
Why?
| | Glucocorticoids | 1 | 2017 | 537 | 0.020 |
Why?
| | Models, Molecular | 1 | 2018 | 1606 | 0.020 |
Why?
| | Cell Line | 1 | 2017 | 2832 | 0.020 |
Why?
| | Cognition | 1 | 2020 | 1286 | 0.020 |
Why?
| | Mental Disorders | 1 | 2021 | 1188 | 0.020 |
Why?
| | Gene Order | 1 | 2011 | 29 | 0.020 |
Why?
| | RNA | 1 | 2017 | 916 | 0.020 |
Why?
| | Reproducibility of Results | 1 | 2019 | 3448 | 0.020 |
Why?
| | Chromosomes, Human, X | 1 | 2011 | 78 | 0.020 |
Why?
| | Chromosomes, Human, Pair 20 | 1 | 2010 | 17 | 0.020 |
Why?
| | Mutagenesis, Insertional | 1 | 2010 | 69 | 0.020 |
Why?
| | Severity of Illness Index | 1 | 2018 | 2973 | 0.020 |
Why?
| | Cell Line, Tumor | 1 | 2017 | 3565 | 0.020 |
Why?
| | Homozygote | 1 | 2010 | 199 | 0.020 |
Why?
| | Age of Onset | 1 | 2011 | 568 | 0.020 |
Why?
| | Phosphotransferases (Phosphate Group Acceptor) | 1 | 2006 | 1 | 0.020 |
Why?
| | Seminal Plasma Proteins | 1 | 2006 | 11 | 0.020 |
Why?
| | Pseudogenes | 1 | 2006 | 20 | 0.020 |
Why?
| | Chromosome Breakage | 1 | 2006 | 23 | 0.020 |
Why?
| | Iran | 1 | 2006 | 44 | 0.020 |
Why?
| | Sperm Motility | 1 | 2006 | 37 | 0.020 |
Why?
| | Creatine Kinase | 1 | 2006 | 72 | 0.020 |
Why?
| | Genes, Recessive | 1 | 2006 | 79 | 0.020 |
Why?
| | Ion Channels | 1 | 2006 | 129 | 0.010 |
Why?
| | Sequence Alignment | 1 | 2006 | 362 | 0.010 |
Why?
| | Amino Acid Sequence | 1 | 2010 | 2134 | 0.010 |
Why?
| | Calcium Channels | 1 | 2006 | 157 | 0.010 |
Why?
| | Protein Tyrosine Phosphatases | 1 | 2006 | 167 | 0.010 |
Why?
| | Intercellular Signaling Peptides and Proteins | 1 | 2006 | 376 | 0.010 |
Why?
| | Haplotypes | 1 | 2006 | 509 | 0.010 |
Why?
| | Nucleic Acid Conformation | 1 | 2006 | 726 | 0.010 |
Why?
| | DNA | 1 | 2010 | 1444 | 0.010 |
Why?
| | Animals | 1 | 2024 | 38410 | 0.010 |
Why?
| | United States | 1 | 2010 | 16313 | 0.010 |
Why?
|
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